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nsv6716815

  • Variant Calls:1
  • Validation:Not tested
  • Clinical Assertions: No
  • Region Size:4,712

    Links to Other Resources

    Source: NCBI

    Genome View

    Select assembly:
    Overlapping variant regions from other studies: 117 SVs from 31 studies. See in: genome view    
    Submitted genomic47,217,351-47,222,062Question Mark
    Overlapping variant regions from other studies: 117 SVs from 31 studies. See in: genome view    
    Remapped(Score: Perfect):47,258,841-47,263,552Question Mark

    Variant Region Placement Information

    Variant Region IDPlacement TypeScoreAssemblyAssembly UnitReciprocitySequence IDChrStartStop
    nsv6716815Submitted genomicGRCh38 (hg38)Primary AssemblyNC_000003.12Chr347,217,35147,222,062
    nsv6716815RemappedPerfectGRCh37.p13Primary AssemblyFirst PassNC_000003.11Chr347,258,84147,263,552

    Variant Call Information

    Variant Call IDTypeMethodAnalysis
    nssv18482766deletionSequencingSplit read and paired-end mapping

    Variant Call Placement Information

    Variant Call IDPlacement TypeScoreHGVSAssemblyReciprocitySequence IDChrStartStop
    nssv18482766Submitted genomicNC_000003.12:g.472
    17351_47222062del
    GRCh38 (hg38)NC_000003.12Chr347,217,35147,222,062
    nssv18482766RemappedPerfectNC_000003.11:g.472
    58841_47263552del
    GRCh37.p13First PassNC_000003.11Chr347,258,84147,263,552

    No validation data were submitted for this variant

    No clinical assertion data were submitted for this variant

    Complete genotype and/or allele frequency data for this study can be found on dbVar's FTP site.

    Genotype Information

    Variant Call IDAllele Frequency (AF)Allele Count (AC)Allele Number (AN)
    nssv184827668.9e-0525275920
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